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Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|January 16, 2008
Non-infectious causes of elevated procalcitonin and C-reactive protein serum levels in pediatric patients with hematologic and oncologic disordersHans Jürgen Dornbusch, Volker Strenger, Petra Sovinz, et al.
Human Mutation|January 1, 1995
Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome)E Popowska, M Rathmann, A Tylki-Szymanska, et al.
Neurology|September 15, 2005
Oculogyric dystonic states in early-onset parkinsonism with basal ganglia calcificationsB Kis, K Hedrich, M Kann, et al.
Journal of Cardiovascular Pharmacology|October 1, 1989
Reduced effects of dopexamine on force of contraction in the failing human heart despite preserved beta 2-adrenoceptor subpopulationM Böhm, B Pieske, P Schnabel, et al.
Journal of Molecular Medicine (Berlin, Germany)|June 13, 1998
Unchanged protein expression of sarcoplasmic reticulum Ca2+-ATPase, phospholamban, and calsequestrin in terminally failing human myocardiumG Münch, B Bölck, S Hoischen, et al.
European Journal of Haematology|July 22, 2006
Long-term use of anagrelide in the treatment of children with essential thrombocythemiaHerwig Lackner, Christian Urban, Martin Benesch, et al.
Pediatric Transplantation|April 14, 2007
Durable remission following a third allogeneic stem cell transplantation in a patient with repeatedly relapsing SAA. The importance of stroma cells for sustained engraftment?Daniela Weber-Mzell, Christian Urban, Martin Benesch, et al.
Medical Physics|May 1, 1988
Modifying constrained least-squares restoration for application to single photon emission computed tomography projection imagesB C Penney, M A King, R B Schwinger, et al.
Human Heredity|January 1, 1989
X-chromosomal DNA polymorphisms in two ethnic groups from IndiaP K Seth, C Meissner, W Kress, et al.
Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Pageof 85

Showing results (481-490 of 849) with videos related to

Sort By:
Pageof 85
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|January 16, 2008
Non-infectious causes of elevated procalcitonin and C-reactive protein serum levels in pediatric patients with hematologic and oncologic disordersHans Jürgen Dornbusch, Volker Strenger, Petra Sovinz, et al.
Human Mutation|January 1, 1995
Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome)E Popowska, M Rathmann, A Tylki-Szymanska, et al.
Neurology|September 15, 2005
Oculogyric dystonic states in early-onset parkinsonism with basal ganglia calcificationsB Kis, K Hedrich, M Kann, et al.
Journal of Cardiovascular Pharmacology|October 1, 1989
Reduced effects of dopexamine on force of contraction in the failing human heart despite preserved beta 2-adrenoceptor subpopulationM Böhm, B Pieske, P Schnabel, et al.
Journal of Molecular Medicine (Berlin, Germany)|June 13, 1998
Unchanged protein expression of sarcoplasmic reticulum Ca2+-ATPase, phospholamban, and calsequestrin in terminally failing human myocardiumG Münch, B Bölck, S Hoischen, et al.
European Journal of Haematology|July 22, 2006
Long-term use of anagrelide in the treatment of children with essential thrombocythemiaHerwig Lackner, Christian Urban, Martin Benesch, et al.
Pediatric Transplantation|April 14, 2007
Durable remission following a third allogeneic stem cell transplantation in a patient with repeatedly relapsing SAA. The importance of stroma cells for sustained engraftment?Daniela Weber-Mzell, Christian Urban, Martin Benesch, et al.
Medical Physics|May 1, 1988
Modifying constrained least-squares restoration for application to single photon emission computed tomography projection imagesB C Penney, M A King, R B Schwinger, et al.
Human Heredity|January 1, 1989
X-chromosomal DNA polymorphisms in two ethnic groups from IndiaP K Seth, C Meissner, W Kress, et al.
Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Pageof 85